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Bone disease in early detected Gaucher Type I disease: A case report
Gaucher disease (GD) is a lysosomal disorder characterized by the storage of glucosylceramide in macrophages (“Gaucher cells”), particularly in the spleen, liver, and bone marrow. The most common phenotype, GD type 1, usually presents with hepatosplenomegaly, cytopenias, and sometimes bone involveme...
Autores principales: | Gragnaniello, Vincenza, Burlina, Alessandro P., Manara, Renzo, Cazzorla, Chiara, Rubert, Laura, Gueraldi, Daniela, Toniolli, Ermanno, Quaia, Emilio, Burlina, Alberto B. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458614/ https://www.ncbi.nlm.nih.gov/pubmed/36101816 http://dx.doi.org/10.1002/jmd2.12314 |
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